ORPHA:98633
OBSOLETE: Goniodysgenesis
inactive · referred to ORPHA:88632Anterior segment developmental anomaly
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Anterior segment developmental anomaly
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Goniodysgenesis | |
| fr | OBSOLETE : Gonio-dysgénésie | |
| de | OBSOLET: Goniodysgenesie | |
| es | OBSOLETO: Goniodisgenesia | |
| it | OBSOLETO: Goniodisgenesia | |
| nl | OBSOLEET: Goniodysgenesie | |
| pt | OBSOLETO: Goniodisgenesia | |
| pl | NIEAKTUALNE: Goniodysgeneza | |
| cs | NEAKTUÁLNÍ: Goniodysgeneze | |
| uk | ЗАСТАРІЛО: Гоніодисгенез | |
| zh | 弃用：前房角发育不全 | |
| tr | Eski adı: Gonyodisgenezi |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98633
- This record as JSON: /data/d/98633.json